Bioorganic & Medicinal Chemistry
基本情報
The Tetrahedron Journal for Research at the Interface of Chemistry and Biology Bioorganic & Medicinal Chemistry publishes complete accounts of research of outstanding significance and timeliness on all aspects of molecular interactions at the interface of chemistry and biology, together with critical review articles. The journal publishes reports of experimental results in medicinal chemistry, chemical biology and drug discovery and design, emphasizing new and emerging advances and concepts in these fields. The aim of the journal is to promote a better understanding at the molecular level of life processes, and living organisms, as well as the interaction of these with chemical agents. The Journal welcomes papers on: the medicinal chemistry and associated biology (including target identification and validation) of established or new disease targets the reporting of the discovery, design or optimization of potent new compounds or biological agents the analysis and discussion of structure-activity relationships and pharmacological issues relevant to drug design and action using in vitro and in vivo models, including the use of computational techniques when closely linked to experimental data the reporting of "first-in-class" new therapeutic compounds the chemical biology or bioorganic/bioinorganic chemistry that significantly advances knowledge of a biological mechanism methodological advances that are chemistry-based and which significantly impact on medicine or biology the preparation and examination of biotherapeutics for the treatment of pathophysiological disease states the development of materials for specific therapeutic targeting All manuscripts will be rigorously peer-reviewed by independent experts following an initial assessment by the Editors. Please note that BMC is not suitable for straightforward reports of incremental advances. Above all the presentation of a rational basis and a sound underlying hypothesis for the work is of particular importance, whatever its exact field.
CiteScore
| 分野 | ランク | パーセンタイル |
|---|---|---|
Pharmacology, Toxicology and PharmaceuticsPharmaceutical Science |
45 / 183 | 75% |
ジャーナル統計
投稿情報
投稿サイト:
https://www.editorialmanager.com/BMCHEM収録タイプ:
Reviews
Perspectives
Symposia-in-Prin
関連論文
Relations between 77Se NMR chemical shifts of (phenylseleno)benzenes and their molecular structures derived from nine X-ray crystal structures
Jette Oddershede, Lars Henriksen, Sine Larsen
DOI: 10.1039/B211130F
Synthetic developments on the preparation of sulfides from thiol-free reagents
Pedro P. de Castro, Juliana A. dos Santos, Troels Skrydstrup, Giovanni W. Amarante
DOI: 10.1039/D0QO01226B
Photochemical synthesis of 3-hydroxyphenanthro[9,10-c]furan-1(3H)-ones from α-keto acids and alkynes
Beibei Zhao, Zhen Zhang, Yu Ge, Pinhua Li, Tao Miao
DOI: 10.1039/D0QO01487G
Substrate-induced DMSO activation and subsequent reaction for rapid construction of substituted pyrimidines
Anan Wang, Xuesong Liu, Yi Kong, Jing Wang, Tao-Shan Jiang
DOI: 10.1039/D0QO01416H
Rational design and syntheses of aniline-based diradical dications: isolable congeners of quinodimethane diradicals
Yong Fang, Qiang Sun, Xiaoyu Chen, Yunfan Qiu, Chao Chen, Lei Wang, Yue Zhao, Yuanting Su, Tao Li, Li Zhang, Xinping Wang
DOI: 10.1039/D0QO01265C
Nitriles as radical acceptors in radical cascade reactions
Kai Sun, Ying-Wu Lin, Bing Yu
DOI: 10.1039/D0QO01058H
(±)-Pinnatifidaones A–D, four pairs of highly modified neolignan enantiomers with a rare spirocyclohexenone skeleton from Crataegus pinnatifida
Rui Guo, Peng Zhao, Xiaoqi Yu, Guodong Yao, Bin Lin, Xiaoxiao Huang, Shaojiang Song
DOI: 10.1039/D0QO01475C
Brønsted acid-catalyzed homogeneous O–H and S–H insertion reactions under metal- and ligand-free conditions
Zhiqin He, Yuxing Xie, Tiantong He, Yaofeng Fu, Yang Yu
DOI: 10.1039/D0QO01401J
Rhodium-catalyzed sequential intermolecular hydroacylation and deconjugative isomerization toward diversified diketones
Zhi-Xin Chang, Jizhong Yan, Chengcai Xia, Fu-Rong Li, Hong-Shuang Li
DOI: 10.1039/D0QO01174F
Rh(iii)-Catalyzed sulfonylamination of α-indolyl alcohols via Csp2–Csp3 bond cleavage
Xinwei Hu, Zheng Tan, Zhipeng Liu, Fengjuan Chen, Huanfeng Jiang, Wei Zeng
DOI: 10.1039/D0QO01426E
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